Airflowing as an adjunctive treatment for periodontitis: A randomized controlled trial

Author:

Alsuwaidi Salem1,Almatrooshi Aisha2,Shah Maanas1,Hakam Abeer1,Tawse‐Smith Andrew3,Alsabeeha Nabeel H. M.4,Atieh Momen A.135ORCID

Affiliation:

1. Mohammed Bin Rashid University of Medicine and Health Sciences Hamdan Bin Mohammed College of Dental Medicine, Dubai Health Dubai United Arab Emirates

2. Dubai Health Dubai United Arab Emirates

3. Sir John Walsh Research Institute, Faculty of Dentistry University of Otago Dunedin New Zealand

4. Department of Dental Services Emirates Health Services Dubai United Arab Emirates

5. School of Dentistry University of Jordan Amman Jordan

Abstract

AbstractBackgoundThe aim of this randomized controlled trial was to assess clinical and patient‐reported outcomes of subgingival instrumentation (SI) with adjunctive use of erythritol airflowing (EAF) compared to SI alone in the treatment of periodontitis.MethodsTwenty‐six participants with Stage III/IV periodontitis requiring nonsurgical periodontal treatment were randomly allocated into two treatment groups: SI with EAF or SI alone. Clinical parameters of percentage of probing pocket depths (PPDs) of ≥5 mm, full mouth bleeding and plaque scores (FMBS and FMPS), and PPD values were recorded at baseline, and at 3 and 6 months posttreatment. A visual analogue scale was used to evaluate postoperative participants’ perception of pain, swelling, bleeding, bruising, and root sensitivity. The impact of periodontal treatment on quality of life was assessed using the General Oral Health Assessment Index (GOHAI) at six months.ResultsA total of 26 participants with Stage III/IV periodontitis completed the 6‐month follow‐up. SI with or without EAF resulted in a statistically significant reductions in the FMBS, FMPS, PPDs, and percentage of PPDs of ≥5 mm at the 3‐ and 6‐month follow‐up visits. There was no statistically significant difference between the two treatment groups for any time interval. Participants receiving SI/EAF exhibited a higher reduction in FMBS compared to those in SI alone group at 3 (SI/EAF: 19.4 ± 11.9, SI alone: 30.1 ± 20.5; P = 0.12) and 6 months (SI/EAF: 14.3 ± 9.6, SI alone: 24.5 ± 18.2; P = 0.09). A lower percentage of sites with deep PPDs (≥5 mm) was also noted amongst participants in the SI/EAF group compared to SI alone at 3 months (SI/EAF: 14.3 ± 14.1, SI alone: 19.2 ± 20.3; P = 0.48) and 6 months (SI/EAF: 8.3 ± 10.0, SI alone: 15.4 ± 17.4; P = 0.22). Patient‐reported outcomes showed no significant differences between the two treatment groups, except in the psychosocial domain of the GOHAI at 6 months favoring the SI/EAF group (P = 0.03).ConclusionsWithin the limitations of the study, the adjunctive use of EAF in addition to SI in the treatment of Stage III/IV periodontitis did not result in a significant improvement in clinical parameters. Limited improvement in the QoL with EAF could be achieved.

Publisher

Wiley

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